EP0510476B1 - Suspensions de polyisocyanate dans des composés réactifs avec des groupes d'isocyanate et leur utilisation - Google Patents

Suspensions de polyisocyanate dans des composés réactifs avec des groupes d'isocyanate et leur utilisation Download PDF

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Publication number
EP0510476B1
EP0510476B1 EP92106347A EP92106347A EP0510476B1 EP 0510476 B1 EP0510476 B1 EP 0510476B1 EP 92106347 A EP92106347 A EP 92106347A EP 92106347 A EP92106347 A EP 92106347A EP 0510476 B1 EP0510476 B1 EP 0510476B1
Authority
EP
European Patent Office
Prior art keywords
suspensions
groups
average
compounds
hydroxyl
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired - Lifetime
Application number
EP92106347A
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German (de)
English (en)
Other versions
EP0510476A1 (fr
Inventor
Werner Drouvé
Peter Dr. Höhlein
Wolfhart Wieczorrek
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Bayer AG
Original Assignee
Bayer AG
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Filing date
Publication date
Application filed by Bayer AG filed Critical Bayer AG
Publication of EP0510476A1 publication Critical patent/EP0510476A1/fr
Application granted granted Critical
Publication of EP0510476B1 publication Critical patent/EP0510476B1/fr
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

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Classifications

    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G18/00—Polymeric products of isocyanates or isothiocyanates
    • C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
    • C08G18/70—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the isocyanates or isothiocyanates used
    • C08G18/72—Polyisocyanates or polyisothiocyanates
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G18/00—Polymeric products of isocyanates or isothiocyanates
    • C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
    • C08G18/28—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
    • C08G18/40—High-molecular-weight compounds
    • C08G18/48—Polyethers
    • C08G18/4891—Polyethers modified with higher fatty oils or their acids or by resin acids
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G18/00—Polymeric products of isocyanates or isothiocyanates
    • C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
    • C08G18/70—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the isocyanates or isothiocyanates used
    • C08G18/703—Isocyanates or isothiocyanates transformed in a latent form by physical means
    • C08G18/705—Dispersions of isocyanates or isothiocyanates in a liquid medium
    • C08G18/707—Dispersions of isocyanates or isothiocyanates in a liquid medium the liquid medium being a compound containing active hydrogen not comprising water
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G18/00—Polymeric products of isocyanates or isothiocyanates
    • C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
    • C08G18/70—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the isocyanates or isothiocyanates used
    • C08G18/72—Polyisocyanates or polyisothiocyanates
    • C08G18/77—Polyisocyanates or polyisothiocyanates having heteroatoms in addition to the isocyanate or isothiocyanate nitrogen and oxygen or sulfur
    • C08G18/78—Nitrogen
    • C08G18/7806—Nitrogen containing -N-C=0 groups
    • C08G18/7818—Nitrogen containing -N-C=0 groups containing ureum or ureum derivative groups
    • C08G18/7825—Nitrogen containing -N-C=0 groups containing ureum or ureum derivative groups containing ureum groups
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G18/00—Polymeric products of isocyanates or isothiocyanates
    • C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
    • C08G18/70—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the isocyanates or isothiocyanates used
    • C08G18/72—Polyisocyanates or polyisothiocyanates
    • C08G18/77—Polyisocyanates or polyisothiocyanates having heteroatoms in addition to the isocyanate or isothiocyanate nitrogen and oxygen or sulfur
    • C08G18/78—Nitrogen
    • C08G18/79—Nitrogen characterised by the polyisocyanates used, these having groups formed by oligomerisation of isocyanates or isothiocyanates
    • C08G18/798—Nitrogen characterised by the polyisocyanates used, these having groups formed by oligomerisation of isocyanates or isothiocyanates containing urethdione groups
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G18/00—Polymeric products of isocyanates or isothiocyanates
    • C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
    • C08G18/70—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the isocyanates or isothiocyanates used
    • C08G18/72—Polyisocyanates or polyisothiocyanates
    • C08G18/80—Masked polyisocyanates
    • C08G18/8003—Masked polyisocyanates masked with compounds having at least two groups containing active hydrogen
    • C08G18/8006—Masked polyisocyanates masked with compounds having at least two groups containing active hydrogen with compounds of C08G18/32
    • C08G18/8038—Masked polyisocyanates masked with compounds having at least two groups containing active hydrogen with compounds of C08G18/32 with compounds of C08G18/3225
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G2190/00—Compositions for sealing or packing joints
    • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10S528/00—Synthetic resins or natural rubbers -- part of the class 520 series
    • Y10S528/903—Polymerizing or processing an isocyanate under substantially anhydrous conditions

Definitions

  • the invention relates to new suspensions of solid, surface-deactivated polyisocyanates in compounds which are reactive towards isocyanate groups and their use for a wide variety of fields of use.
  • the invention relates to storage-stable at room temperature, thermosetting, optionally auxiliary and Additives of coating technology containing suspensions of solid polyisocyanates deactivated on the surface by adduct formation in organic compounds with at least two groups which are reactive towards isocyanate groups as a continuous phase, characterized in that the compounds forming the continuous phase are composed of at least 10% by weight of ether and Polyhydroxyl compounds containing ester groups have an (average) hydroxyl functionality of 0.5 to 3 and an (average) hydroxyl number of 15 to 150 and the esterification product of (i) polyether polyols with an (average) hydroxyl functionality of 3 to 8 and an (average) hydroxyl number of 200 to 1000 with (ii) represent 40 to 90 equivalent% of organic monocarboxylic acids, the percentages relating to the hydroxyl groups of component (i) and the carboxyl groups of component (ii).
  • the invention also relates to the use of the suspensions according to the invention for the production of yellowing-resistant, heat-curable coatings, bonds or sealing compounds for any substrates, in particular as underbody and sill protection compounds for motor vehicles.
  • the suspensions according to the invention essentially consist of finely divided solid polyisocyanates, deactivated on the surface, as a disperse phase and liquid at room temperature with respect to isocyanate groups reactive organic compounds having groups as a continuous phase.
  • the dispersions according to the invention can of course also contain auxiliaries and additives, as are known, for example, from coating technology. These additives can either be solid substances so that they are part of the disperse phase (for example pigments or fillers) or they can also be soluble substances so that they are part of the continuous phase (for example plasticizers, catalysts and the like).
  • the main constituent of the disperse phase solid, finely divided polyisocyanates which are deactivated on the surface, correspond to the compounds of the prior art hitherto used for this purpose.
  • Particularly preferred deactivating agents are primary and / or secondary amines with (cyclo) aliphatically bound amino groups, such as, in particular, ethylenediamine, hexamethylene diamine, 4,4'-diamino-dicyclohexylmethane or in particular 4,4'-diamino-3,3'-dimethyl-dicyclohexylmethane.
  • the deactivation can take place both in situ in the polyhydroxyl compounds or part of the polyhydroxyl compounds which form the essential constituent of the continuous phase of the suspensions according to the invention, or else in a separate batch using organic liquids which are suitable for the deactivating agent but not for the solid starting polyisocyanate represent a solvent, for example in acetone or cyclohexane, as described in EP-A-0 062 780. Water is also suitable as a reaction medium for the deactivation reaction.
  • the aminic deactivating agent is used in an amount of 0.01 to 25, preferably 0.1 to 8 and particularly preferably 0.3 to 3 equivalent%, based on the amino groups of the deactivating agent and the isocyanate groups of the suspended starting polyisocyanate. Otherwise, the deactivation takes place in complete analogy to the processes already known, for example described in the publications mentioned above.
  • the chemical nature of the polyhydroxyl compounds used as a continuous phase is essential to the invention.
  • the continuous phase of the suspensions according to the invention consists of at least 10% by weight of polyhydroxyl compounds of the type already mentioned which contain ether and ester groups.
  • These polyhydroxyl compounds which are essential to the invention are preferably those having an (average) hydroxyl functionality of 0.5 to 3 and a ( average) hydroxyl number from 15 to 150 with a viscosity of 150 to 350 mPa.s / 20 ° C.
  • polyhydroxyl compounds which are essential to the invention and have ether and ester groups
  • other compounds known per se from polyurethane chemistry with groups which are reactive toward isocyanate groups may be present in the continuous phase of the suspensions according to the invention.
  • Both alcoholic hydroxyl groups and primary or secondary amino groups which are at least difunctional in the sense of the isocyanate addition reaction of the type known per se are suitable.
  • Polyhydroxy polyesters, polyethers, polycarbonates or polyacetals known from polyurethane chemistry and having a molecular weight in the range from 400 to 6000, preferably 800 to 6000 and particularly preferably 1000 to 4500 with 2 to 8, preferably 2 to 4, hydroxyl groups per molecule, derived from polyurethane chemistry, may be mentioned as examples known amino polyethers of a corresponding molecular weight range with preferably 2 to 4 primary, aliphatically or aromatically bound amino groups or also low molecular chain extenders or crosslinking agents such as, for example, polyhydric alcohols of the molecular weight range 62 to 400 such as ethylene glycol, glycerol, trimethylolpropane, pentaerythritol, the low molecular weight alkoxylation aliphatic alkoxylation products of these Polyamines like Ethylene diamine or hexamethylene diamine, cycloaliphatic polyamines such as 4,4'-diamino-dicyclohe
  • the powdery solid polyisocyanates which are deactivated on the surface are present in an amount which corresponds to an equivalent ratio of isocyanate groups from stabilized isocyanate to amino or hydroxyl groups of the continuous phase of 0.5: 1 to 1.5: 1, preferably correspond to 0.8: 1 to 1.5: 1, with (dimeric) diisocyanates containing uretdione groups only being included in the calculation with regard to the free isocyanate groups present in them.
  • the suspensions according to the invention may contain the auxiliaries and additives known per se from lacquer technology, such as, for example, pigments, fillers, catalysts, flow or rheology aids, inert solvents or plasticizers.
  • auxiliaries and additives known per se from lacquer technology, such as, for example, pigments, fillers, catalysts, flow or rheology aids, inert solvents or plasticizers.
  • the suspensions according to the invention are comparatively low-viscosity systems which can be applied by the customary methods of coating technology.
  • the suspensions are suitable as coating agents, adhesive agents, anti-drumming agents or seam sealing compounds on metals or non-metals. They are particularly preferably used as underbody protection and sill protection compositions for motor vehicles. They are generally cured by heating at 110 to 150 ° C. for 15 to 40 minutes.
  • the column is first removed and then the nitrogen flow is increased to 30 l / hour. It is condensed until an acid number of 1.4 mg KOH / g substance has been reached. The mixture is then cooled to 100 ° C. and the finished product is filtered through a fabric filter.
  • the result is a polyhydroxyl compound which can be used according to the invention with an iodine color number of 2, a viscosity of 225 mPasec at 20 ° C., an OH number of 23 mg KOH / g substance and an acid number of 4.5 mg KOH / g substance.
  • Example 2 The procedure is as in Example 1, but 6 852 g of soybean oil fatty acid and 4 586 g of the propoxylated sorbitol are weighed out. The result is a polyhydroxyl compound which can be used according to the invention with an iodine color number of 2, a viscosity of 280 mPa.s at 23 ° C., an OH number of 66 mg KOH / g substance and an acid number of 1.7 mg KOH / g substance.
  • Coating compositions corresponding to Examples 4 to 6 were applied to a pre-primed steel sheet in a layer thickness of approximately 550 ⁇ m and cured at 120 ° C. for 30 minutes.
  • the product properties relevant for use in the underbody or sill protection area are compared in tabular form below. The comparison data make it clear that the system according to the invention has considerable advantages over the comparison example both in terms of the application viscosity, in the surface properties and in the yellowing behavior.

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  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Organic Chemistry (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Dispersion Chemistry (AREA)
  • Polyurethanes Or Polyureas (AREA)
  • Paints Or Removers (AREA)
  • Sealing Material Composition (AREA)
  • Adhesives Or Adhesive Processes (AREA)
  • Vehicle Waterproofing, Decoration, And Sanitation Devices (AREA)
  • Seal Device For Vehicle (AREA)

Claims (3)

  1. Suspensions stables à la conservation à la température ambiante, durcissables à la chaleur, contenant le cas échéant des produits auxiliaires et additifs de l'industrie des peintures et vernis, de polyisocyanates solides, désactivés en surface par formation d'adducts, dans des composés organiques contenant au moins deux groupes réactifs avec les groupes isocyanates et qui constituent la phase continue, caractérisées en ce que les composés formant la phase continue consistent pour au moins 10 % en poids en composés polyhydroxylés contenant des groupes éthers et esters, à une fonctionnalité (moyenne) en groupes hydroxy de 0,5 à 3 et un indice d'hydroxyle (moyen) de 15 à 150 et sont des produits d'estérification de (i) des polyétherpolyols à une fonctionnalité (moyenne) en groupes hydroxy de 3 à 8 et un indice d'hydroxyle (moyen) de 200 à 1 000, avec (ii) 40 à 90 équivalents% d'acides organiques monocarboxyliques, les pourcentages indiqués se rapportant aux groupes hydroxy du composant (i) et aux groupes carboxyle du composant (ii).
  2. Utilisation des suspensions selon revendication 1 pour l'application de revêtements, la réalisation de collages ou la préparation de masses d'étanchéité résistant au jaunissement, durcissables sous l'action de la chaleur, pour des supports quelconques.
  3. Utilisation des suspensions selon revendication 1 en tant que masses de protection pour dessous de plancher et traverses de véhicule.
EP92106347A 1991-04-25 1992-04-13 Suspensions de polyisocyanate dans des composés réactifs avec des groupes d'isocyanate et leur utilisation Expired - Lifetime EP0510476B1 (fr)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
DE4113416 1991-04-25
DE4113416A DE4113416A1 (de) 1991-04-25 1991-04-25 Polyisocyanatsuspensionen in gegenueber isocyanatgruppen reaktionsfaehigen verbindungen und ihre verwendung

Publications (2)

Publication Number Publication Date
EP0510476A1 EP0510476A1 (fr) 1992-10-28
EP0510476B1 true EP0510476B1 (fr) 1995-11-15

Family

ID=6430277

Family Applications (1)

Application Number Title Priority Date Filing Date
EP92106347A Expired - Lifetime EP0510476B1 (fr) 1991-04-25 1992-04-13 Suspensions de polyisocyanate dans des composés réactifs avec des groupes d'isocyanate et leur utilisation

Country Status (7)

Country Link
US (1) US5185422A (fr)
EP (1) EP0510476B1 (fr)
JP (1) JPH07179563A (fr)
KR (1) KR920019838A (fr)
CA (1) CA2066482A1 (fr)
DE (2) DE4113416A1 (fr)
ES (1) ES2081513T3 (fr)

Families Citing this family (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE4327573A1 (de) * 1993-08-17 1995-02-23 Bayer Ag Uretdion-Pulverlackvernetzer mit niedriger Schmelzviskosität
DE4407490A1 (de) * 1994-03-07 1995-09-14 Bayer Ag Verfahren zur Herstellung heißhärtender Einkomponenten-Polyurethan-Reaktivmassen
DE19723355A1 (de) * 1997-06-04 1998-12-10 Sika Chemie Gmbh Verfahren zur Herstellung von einkomponentigen Dichtungs- und Beschichtungsmassen auf Polyurethanbasis
DE19846650A1 (de) 1998-10-09 2000-04-13 Basf Coatings Ag Pulverlack-Slurry mit mikroverkapselten Partikeln, ihre Herstellung und ihre Verwendung
DE19924138A1 (de) 1999-05-26 2000-11-30 Henkel Kgaa Lösbare Klebeverbindungen
DE19951599A1 (de) * 1999-10-27 2001-05-23 Henkel Kgaa Verfahren zur adhesiven Trennung von Klebeverbunden
DE10001442A1 (de) * 2000-01-15 2001-10-18 Basf Coatings Ag Strukturviskose, von organischen Lösemitteln freie Pulverklarlack-Slurry, Verfahren zu ihrer Herstellung und ihre Verwendung
DE10037884A1 (de) 2000-08-03 2002-02-21 Henkel Kgaa Verfahren zur beschleunigten Klebstoffaushärtung
DE10040223C2 (de) * 2000-08-17 2002-12-05 Basf Coatings Ag Strukturviskose, von organischen Lösemitteln und externen Emulgatoren freie Pulverklarlack-Slurry, Verfahren zu ihrer Herstellung und ihre Verwendung
ATE376015T1 (de) * 2002-12-23 2007-11-15 Dow Global Technologies Inc Reaktive polyurethanzusammensetzung

Family Cites Families (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE3112054A1 (de) * 1981-03-27 1982-10-07 Basf Ag, 6700 Ludwigshafen Lagerstabile, hitzhaertbare stoffmischungen aus polyisocyanat und polyol, verfahren zu deren herstellung und verwendung
DE3230757A1 (de) * 1982-08-18 1984-02-23 Bayer Ag, 5090 Leverkusen Verfahren zur herstellung von stabilisierten polyisocyanaten, stabilisierte polyisocyanate retardierter reaktivitaet und ihre verwendung zur polyurethanherstellung
DE3418430A1 (de) * 1984-05-18 1985-11-21 Bayer Ag, 5090 Leverkusen Verfahren zur herstellung desaktivierter suspensionen von feinteiligen polyisocyanaten in hoehermolekularen verbindungen, desaktivierte suspensionen und ihre verwendung zur polyurethanherstellung
DE3526790A1 (de) * 1985-07-26 1987-01-29 Bayer Ag Ether- und ethergruppen aufweisende polyhydroxylverbindungen und ihre verwendung als aufbaukomponente bei der herstellung von polyurethankunststoffen, insbesondere als polyolkomponente in polyurethan-beschichtungsmitteln oder -vergussmassen
DE3638148A1 (de) * 1986-11-08 1988-05-11 Bayer Ag Verfahren zur herstellung von feinteiligen harnstoffgruppen enthaltenden polyisocyanaten

Also Published As

Publication number Publication date
JPH07179563A (ja) 1995-07-18
ES2081513T3 (es) 1996-03-16
US5185422A (en) 1993-02-09
DE59204298D1 (de) 1995-12-21
DE4113416A1 (de) 1992-10-29
EP0510476A1 (fr) 1992-10-28
KR920019838A (ko) 1992-11-20
CA2066482A1 (fr) 1992-10-26

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